BEUDAMED
    9 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·September 4, 2019

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·January 20, 2018

    BD PHASEAL¿ INJECTOR LUER LOCK N35

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·June 12, 2023

    BD PHASEAL¿ INJECTOR LUER LOCK N35

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·June 13, 2023

    MAXCEM ELITE

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code EMA·May 13, 2013

    CYLOS DR

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code DXY·September 23, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·April 28, 2011

    BD WHITACRE¿ SPINAL NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·August 7, 2023

    BD 5ML LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·September 3, 2019